Pages that link to "Hyperprolinemia"
The following pages link to Hyperprolinemia:
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Tyrosinemia (← links | edit)
- Trimethylaminuria (← links | edit)
- List of diseases (H) (← links | edit)
- Glutamate receptor (← links | edit)
- Glutathione synthetase deficiency (← links | edit)
- Guanidinoacetate methyltransferase deficiency (← links | edit)
- Hyperlysinemia (← links | edit)
- Hypermethioninemia (← links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links | edit)
- Ornithine translocase deficiency (← links | edit)
- Prolidase deficiency (← links | edit)
- Sarcosinemia (← links | edit)
- Succinic semialdehyde dehydrogenase deficiency (← links | edit)
- Urea cycle disorder (← links | edit)
- Inborn error of metabolism (← links | edit)
- Proline (← links | edit)
- List of amino acid metabolism disorders (← links | edit)
- Methylmalonyl-CoA mutase deficiency (← links | edit)
- Template:Amino acid metabolic pathology (← links | edit)
- Inborn errors of renal tubular transport (← links | edit)
- Hypervalinemia (← links | edit)
- Organic acidemia (← links | edit)
- Carnosinemia (← links | edit)
- Hawkinsinuria (← links | edit)
- Inborn errors of amino acid metabolism (← links | edit)
- D-Glyceric acidemia (← links | edit)
- Urocanic aciduria (← links | edit)
- Amino acid transport disorder (← links | edit)
- Argininemia (← links | edit)
- 2-Hydroxyglutaric aciduria (← links | edit)
- Proline oxidase (← links | edit)
- Prolinemia (redirect page) (← links | edit)
- Prolinuria (redirect page) (← links | edit)
- Type I tyrosinemia (← links | edit)
- Type II tyrosinemia (← links | edit)
- Type III tyrosinemia (← links | edit)
- User:Justindchien/New Glutamate Receptor Page (← links | edit)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links | edit)
- Hypertryptophanemia (← links | edit)
- Aldehyde dehydrogenase 4 family, member A1 (← links | edit)
